PCIDB

KNApSAcK Metabolite C00002172

Metabolite

KNApSAcK Entry

id C00002172
Name Haplopine
CAS RN 5876-17-5
Standard InChI InChI=1S/C13H11NO4/c1-16-11-7-3-4-9(15)12(17-2)10(7)14-13-8(11)5-6-18-13/h3-6,15H,1-2H3
Standard InChI (Main Layer) InChI=1S/C13H11NO4/c1-16-11-7-3-4-9(15)12(17-2)10(7)14-13-8(11)5-6-18-13/h3-6,15H,1-2H3

Cluster

Phytochemical cluster No. 7
KCF-S cluster No. 368

Link

ChEMBL

By standard InChI CHEMBL455007
By standard InChI Main Layer CHEMBL455007

KEGG

By LinkDB C10694

CTD

By CAS RN C012345

Human Protein / Gene in interaction

3 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P55789 FAD-linked sulfhydryl oxidase ALR Enzyme CHEMBL455007 CHEMBL1738573 (1)
1 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein CHEMBL455007 CHEMBL2114810 (1)
7 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme CHEMBL455007 CHEMBL1613914 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#174800 Mccune-albright syndrome; mas P63092
#613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay P55789
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092

KEGG DISEASE (3)

KEGG disease name UniProt
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)